| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132362160-132362218 | Rare:8 | ||||
| chr6:132378579-132378859 | Common:1; Rare:50 | ||||
| chr6:132379260-132379655 | Common:2; Rare:66 | ||||
| chr6:132380418-132380436 | Rare:7 | ||||
| chr6:132394780-132395023 | Common:2; Rare:39 | ||||
| chr6:132402688-132402943 | Common:2; Rare:41 | ||||
| chr6:132816465-132816924 | Common:1; Rare:163 | ||||
| chr6:134296035-134296328 | Common:2; Rare:50 | ||||
| chr6:134348623-134348738 | Common:1; Rare:16 | ||||
| chr6:135358170-135358313 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr6:139578421-139578510 | Rare:19 | ||||
| chr6:140602329-140602528 | Rare:34 | ||||
| chr6:140602984-140602999 | Rare:4 | ||||
| chr6:140606508-140606651 | Rare:27 | ||||
| chr6:140609830-140610330 | Common:3; Rare:95 |